Question:

Convert the following: 
i. Ethyl alcohol into ethyl acetate 
ii. Phenol into benzene 
iii. Diethyl ether into ethyl chloride

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Choose reagents specific to functional group transformations for efficient organic conversions.
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Solution and Explanation

i. Ethyl Alcohol to Ethyl Acetate: 

CH3CH2OH + CH3COOH ⟶H2SO4, heat CH3COOCH2CH3 + H2O

Explanation: Ethyl alcohol reacts with acetic acid in the presence of concentrated sulphuric acid and heat to form ethyl acetate (an ester) and water. This reaction is known as **esterification**.


ii. Phenol to Benzene:

C6H5OH ⟶Zn dust, heat C6H6 + ZnO

Explanation: When phenol is heated with zinc dust, it undergoes reduction. The –OH group is removed as ZnO and the product formed is **benzene**.


iii. Diethyl Ether to Ethyl Chloride:

(C2H5)2O + 2HCl ⟶ZnCl2, heat 2C2H5Cl + H2O

Explanation: Diethyl ether reacts with concentrated hydrochloric acid in the presence of anhydrous zinc chloride upon heating to form **ethyl chloride** and water. This is an example of **cleavage of ether** by halogen acids.


Topic: Alcohols, Phenols, and Ethers — Conversion Reactions

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